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QUINCKE SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K022029
510(k) Type
Traditional
Applicant
EPIMED INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2002
Days to Decision
39 days
Submission Type
Summary

QUINCKE SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K022029
510(k) Type
Traditional
Applicant
EPIMED INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2002
Days to Decision
39 days
Submission Type
Summary